| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31094574-31094817 | Common:1; Rare:92; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr16:31108317-31108471 | Rare:41 | ||||
| chr16:31202716-31202943 | Common:2; Rare:78 | ||||
| chr16:31442787-31443059 | Common:1; Rare:42 | ||||
| chr16:31459086-31459137 | Rare:15 | ||||
| chr16:31459296-31459503 | Common:1; Rare:87 | ||||
| chr16:31471896-31472189 | Rare:65 | ||||
| chr16:31508374-31508508 | Common:4; Rare:55 | ||||
| chr16:46689129-46689416 | Common:1; Rare:102; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689518-46689708 | Common:2; Rare:79; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46973581-46973801 | Rare:100 | ||||
| chr16:47461005-47461383 | Common:2; Rare:155; Clinvar (benign):2 | ||||
| chr16:48244254-48244482 | Common:2; Rare:71 | ||||
| chr16:49281742-49282137 | Common:2; Rare:121 | ||||
| chr16:49282214-49282554 | Common:4; Rare:79 |